EP3522904B1 - Composition liquide destinée à être utilisée dans le traitement de reflux gastro-oesophagien - Google Patents

Composition liquide destinée à être utilisée dans le traitement de reflux gastro-oesophagien Download PDF

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Publication number
EP3522904B1
EP3522904B1 EP17797183.5A EP17797183A EP3522904B1 EP 3522904 B1 EP3522904 B1 EP 3522904B1 EP 17797183 A EP17797183 A EP 17797183A EP 3522904 B1 EP3522904 B1 EP 3522904B1
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EP
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Prior art keywords
composition
honey
aloe vera
vera gel
salt
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EP17797183.5A
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German (de)
English (en)
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EP3522904A1 (fr
Inventor
Andrea BIFFI
Sara SALA
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Sofar Swiss SA
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Sofar Swiss SA
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/56—Materials from animals other than mammals
    • A61K35/63—Arthropods
    • A61K35/64—Insects, e.g. bees, wasps or fleas
    • A61K35/644—Beeswax; Propolis; Royal jelly; Honey
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
    • A61K31/728—Hyaluronic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/737—Sulfated polysaccharides, e.g. chondroitin sulfate, dermatan sulfate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18—Magnoliophyta (angiosperms)
    • A61K36/88—Liliopsida (monocotyledons)
    • A61K36/886—Aloeaceae (Aloe family), e.g. aloe vera
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants

Definitions

  • the present invention relates to a liquid composition for use in the treatment of gastroesophageal reflux, preferably an aqueous liquid composition.
  • the composition of the present invention preferably in the form of an aqueous liquid composition, comprises a mixture which comprises or, alternatively, consists of a combination of Aloe vera gel, hyaluronic acid and honey and, optionally, food or pharmaceutical grade additives and/or technological excipients.
  • composition of the present invention also relates to a medical device comprising a mixture which comprises or, alternatively, consists of a combination of Aloe vera gel, hyaluronic acid and honey and, optionally, food or pharmaceutical grade additives and/or technological excipients.
  • Said composition or composition for a medical device being for use in the preventive and/or curative treatment of the symptoms associated with gastroesophageal reflux and the disease caused thereby, as well as for use in the preventive and/or curative treatment of gastroesophageal reflux disorders.
  • Gastroesophageal reflux is a phenomenon characterised by the temporary upflow of stomach contents into the esophagus, without there necessarily being regurgitation or vomiting.
  • the reflux is principally due to releases of the lower esophageal sphincter (LES), which can be due to insufficient pressure of the LES relative to an increase in abdominal pressure, or a progressive weakening of the closing pressure.
  • LES lower esophageal sphincter
  • Gastroesophageal reflux disease abbreviated as GERD (or GORD, gastro-oesophageal reflux disease), is a chronic disease of gastroenterological interest, which is linked to pathological complications of gastroesophageal reflux (GER) and consists in damage to the mucosa of the esophagus caused by gastric acid.
  • GORD gastro-oesophageal reflux disease
  • GERD GERD GERD
  • GERD can bring about permanent damage to the esophagus, such as chronic inflammation and necrosis of the esophageal epithelium (esophagitis), ulcers, esophageal stenosis, Barrett's esophagus, which is a form of metaplasia characterised by a replacement of the squamous epithelium typical of the esophagus with a cylindrical epithelium, and tumours.
  • Subjects with persistent symptoms of GERD are considered to be at high risk of developing adenocarcinoma of the distal tract of the esophagus.
  • An assessment of the damage to the esophageal mucosa is generally performed by means of endoscopic examinations, e.g. gastroscopy or pH-metry.
  • the administration of these drugs can be ineffective in some subjects and can have side effects at the intestinal level (diarrhoea, flatulence, abdominal pain), skin eruptions, heart palpitations and an increase in osteoporosis and bone fragility in the case of long-term treatments.
  • the present invention provides a composition, comprising substances of natural origin, which is capable of treating (preventing and/or curing) the symptoms associated with gastroesophageal reflux, and the disease caused thereby, and which is practically devoid of the side effects that are present in the prior art treatments.
  • the present invention relates to a liquid composition (C) comprising a mixture which comprises or, alternatively, consists of a combination of the following substances:
  • the liquid composition (C) is for use in the treatment of gastroesophageal reflux and is in the form of an aqueous liquid composition. It has been found that the administration of a mixture which comprises or, alternatively, consists of a combination of the three substances (a), (b) and (c) is capable of considerably decreasing/reducing and/or eliminating the symptoms and disorders associated with gastroesophageal reflux, alleviating the effects of the disease itself.
  • the liquid composition (C) of the present invention acts along the esophagus and performs an anti-inflammatory and cicatrising action against the lesions caused to the mucosa as a result of the upflow of vapours and acidic substances or substances of an acidic character from the stomach towards the esophagus.
  • the liquid composition (C) of the present invention enables better contact of the individual components/substances contained in the mixture with the oral-pharyngeal-laryngeal-esophageal wall and favours the protection, lubrication and repair thereof.
  • composition (C) according to the present invention can be in the form of a clear solution (i.e. without precipitates) or suspension (i.e. a liquid phase that exhibits a visible opalescence, a solid suspended in a liquid or semi-liquid mass or a precipitate that can be suspended under stirring) and it can be a dense viscous liquid (like caramel) or a flowable fluid (like water) or it can be a two-phase liquid/liquid system.
  • a clear solution i.e. without precipitates
  • suspension i.e. a liquid phase that exhibits a visible opalescence, a solid suspended in a liquid or semi-liquid mass or a precipitate that can be suspended under stirring
  • it can be a dense viscous liquid (like caramel) or a flowable fluid (like water) or it can be a two-phase liquid/liquid system.
  • the composition of the present invention is in the form of a syrup, for example having a specific weight of about 1.2-1.3 kg/dm 3 at 20°C and a viscosity of about 200-205 mPa.s at 20°C, comprising water and at least one food or pharmaceutical grade ingredient or additive and/or technological excipients.
  • treatment means an intervention, comprising the administration of a substance, or mixture of substances or combination thereof, having the aim of eliminating, reducing/decreasing or preventing a pathology or disease and the symptoms or disorders associated therewith.
  • contents of a component or substance in a composition refers to the percentage by weight of that component or substance relative to the total weight of the composition.
  • compositions comprising one or more components or substances means that other components or substances can be present in addition to the one or ones specifically indicated.
  • composition of the present invention is to be understood as for either human or veterinary use, i.e. as a preparation to be applied to animals with the uses and methods known to the person skilled in the art.
  • treatment means an intervention comprising the administration of a substance, or mixture of substances, having the aim of eliminating, reducing or preventing a pathology and the symptoms thereof.
  • honey means the sweet natural product produced by bees (e.g. Apis mellifera ) from the nectar of one or more plant varieties of any type or from secretions originating from living parts of plants or substances secreted by sucking insects that are found on living parts of plants, which they collect, transform, by combining them with specific substances of their own, deposit, dehydrate, store and leave in honeycombs to ripen and mature, according to the definition in Italian Legislative Decree no. 179 of 21 May 2004, transposing Directive 2001/110/EC relating to the production and marketing of honey.
  • bees e.g. Apis mellifera
  • honey can be obtained through the standard processes known to the person skilled in the art (for example comprising extraction, separation, decanting, filtration, guided crystallisation and similar operations).
  • the term "honey” also comprises the products that can be obtained from natural honey, including those for industrial use, for example through refining processes or heat treatments, such as pasteurisation.
  • Patent EP 1 230 742 B1 describes the use of honey having a peroxide activity greater than 5 micrograms of hydrogen peroxide per gram of honey, in combination with crude food fibres (such as wheat bran), for the production of a composition for combating disorders such as gastroesophageal reflux.
  • the honey usable in the composition of the present invention can have a pH between 3.5 and 4.5 (by weight relative to the total weight of the honey), a weight loss on drying of 18% and a content of reducing sugars in the dry product of 70%.
  • Aloe vera gel means the generally colourless mucilaginous gel obtained from the parenchymatous tissue of the leaves of Aloe vera (L) Burm. f. or Aloe barbadensis Mill. Aloe vera gel does not have a use as a food substance or fibre and must not be confused with the juice, which is obtained from the same plant by incision and drying. In the monograph on Aloe vera gel in " WHO monographs on selected medicinal plants” (Vol. 1 World Health Organization, Geneva, 1999 pp.
  • the present inventors have found, by contrast, that oral administration of Aloe vera gel, in combination with honey and hyaluronic acid, in accordance with the present invention, enables the symptoms and disorders associated with gastroesophageal reflux to be considerably decreased or completely eliminated.
  • the Aloe vera gel is lyophilised inner leaf gel, more preferably from Aloe barbadensis Miller.
  • the Aloe vera gel used in the present invention can have a pH between 3 and 6, preferably between 3.5 and 5.5 or 3.7 and 4.2, and have a content of aloin lower than 1 ppm.
  • Hyaluronic acid is a non-sulphated glycosaminoglycan having an unbranched polysaccharide chain deriving from the condensation of disaccharide units which are formed, in turn, from residues of glucuronic acid and N-acetylglucosamine, linked together by alternating glycosidic bonds ⁇ 1 ⁇ 4 and ⁇ 1 ⁇ 3 (CAS number 9004-61-9).
  • Hyaluronic acid is widely used also in the form of a salt, for example as a sodium salt, via injections, in aesthetic surgery and dermatology, in otologic surgery, in ophthalmic surgery and in arthrology. Moreover, hyaluronic acid is widely used for topical application against inflammations or ulcerous lesions of the mouth and as a filler for skin applications in facial and body care products.
  • the hyaluronic acid can be in the acid or salt form, for example as a sodium salt; the hyaluronic acid is preferably in linear form.
  • the mixture contained in the composition (C) according to the present invention may comprise hyaluronic acid, or salts thereof, having a different origin and various intervals of molecular weights.
  • the hyaluronic acid, or salts thereof, used in the mixture contained in the composition (C) of the present invention, in combination with the substances (a) and (c) and/or (d), is linear or branched; the hyaluronic acid is preferably in linear form.
  • the mixture contained in said composition (C) according to the present invention comprises linear or branched hyaluronic acid, or salts thereof, having molecular weight comprised from 400 to 900 kDa, preferably from 600 to 800 kDa; the hyaluronic acid is preferably in linear form.
  • the mixture contained in said composition (C) according to the present invention comprises sodium hyaluronate having a molecular weight comprised from 600 to 800 kDalton (CAS No. 9067-32-7).
  • composition (C) of the present invention further comprises at least one other glycosaminoglycan (GAG), or a salt thereof, in addition to the hyaluronic acid; more preferably, said GAG is a salt of chondroitin; even more preferably, said GAG is the substance (d) chondroitin sulphate.
  • GAG glycosaminoglycan
  • the chains of chondroitin, or of the derivatives thereof such as sulphate are branchless polysaccharides of variable length containing two alternating monosaccharides: D-glucuronic acid (GlcA) and N-acetyl-D-galactosamine (GalNAc), wherein the residues of GlcA can be epimerised into L-iduronic acid (the resulting disaccharide is called Dermatan sulphate).
  • chondroitin sulphate is a generic term that indicates a polymer having an average molecular weight of about 50,000 Da.
  • chondroitin sulphate such as, for example, chondroitin 4-sulphate A [ CAS No. 24967-93-9 ], the sodium salt thereof [ CAS No. 9082-07-9 ] or the disodium salt thereof [ CAS No. 39455-18-0 ].
  • the form chondroitin 6-sulphate (chondroitin sulphate C) also exists- CAS No. 25322-46-7 .
  • chondroitin sulphate (d) in combination with the substances (a), (b) and (c) and said chondroitin (d) is chicken chondroitin.
  • the chondroitin sulphate (optionally in the form of a sodium salt) in the composition for use according to the present invention has an average molecular weight that depends on the specific form of chondroitin used.
  • liquid composition (C) according to the invention also comprising chondroitin sulphate, has the effect of further reducing the symptoms associated with gastroesophageal reflux, practically in the absence of undesirable effects.
  • the chondroitin sulphate in the composition (C) of the invention preferably derives from chicken, fish (e.g. shark chondroitin sulphate, CAS number 9082-07-9), bovines or swine or is of vegetable origin; more preferably, the chondroitin sulphate, or salts thereof, used in the composition of the present invention derives from chicken.
  • fish e.g. shark chondroitin sulphate, CAS number 9082-07-9
  • bovines or swine or is of vegetable origin
  • the chondroitin sulphate, or salts thereof, used in the composition of the present invention derives from chicken.
  • the chondroitin sulphate in the composition according to the present invention may be chicken chondroitin sulphate sodium salt and contain, relative to the total weight of chondroitin sulphate sodium salt, at least 91.5% by weight of chondroitin sulphate and no more than 8.5% by weight of sodium, it may have a protein content no greater than 6% by weight and have a pH comprised from 5.5 to 7.5 and/or a specific rotation comprised from 10° to 20° (for example determined with the methods of the European Pharmacopoeia 7.0).
  • liquid composition (C) comprises a mixture which comprises or, alternatively, consists of:
  • liquid composition (C) of the present invention comprises, per 100 ml of (C):
  • liquid composition (C) comprises, per 100 ml of (C):
  • liquid composition (C) comprises, per 100 ml of (C):
  • liquid composition (C) according to the present invention in addition to the component (a)-(c) and, optionally, (d), can further comprise other active ingredients such as, by way of non-limiting example, anti-inflammatory agents, oral cavity disinfectants, antacids and mixtures thereof.
  • composition (C) as defined above can further comprise at least one excipient, or additive, i.e. a substance devoid of therapeutic activity, suitable for pharmaceutical or food use.
  • the acceptable ingredients for pharmaceutical or food use comprise all the auxiliary substances known to the person skilled in the art and suitable for the preparation of liquid forms for oral administration, such as, by way of non-limiting example, diluents, solvents (including water, glycerine, ethyl alcohol), solubilisers, thickeners, sweeteners, flavourings, colourants, lubricants, surfactants, antimicrobials, antioxidants, preservatives, pH stabilising buffers and mixtures thereof.
  • diluents including water, glycerine, ethyl alcohol
  • solubilisers such as, sweeteners, flavourings, colourants, lubricants, surfactants, antimicrobials, antioxidants, preservatives, pH stabilising buffers and mixtures thereof.
  • Non-limiting examples of such substances are maltodextrins, phosphate buffers, bases such as sodium hydroxide, xanthan gum, guar gum, fructose, and natural or artificial flavouring
  • the present invention provides a medical device comprising the composition (C) as defined above.
  • the term "medical device” is used with the meaning according to Italian Legislative Decree no. 46 of 24 February 1997, i.e. it indicates a substance or another product, whether used alone or in combination, intended by the manufacturer to be used for human beings for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease, and which does not achieve its principal intended action in or on the human body for which it is intended by pharmacological, immunological or metabolic means, but which may be assisted in its function by such means.
  • said medical device can be in the form of a syrup, liquid or semi-solid preparation, gel, suspension, solution, two-phase liquid system and equivalent forms.
  • the medical device according to the invention is in the form of a syrup.
  • the present invention provides a composition comprising a mixture or an association or a combination which comprises or, alternatively, consists of:
  • (a), (b) and (c) can be also administered separately and in any order but, preferably, (a), (b) and (c) are administered to a subject simultaneously, and even more preferably in a single composition so as to obtain a more rapid effect and facilitate administration.
  • said combination according to the present invention further comprises a salt of chondroitin, preferably of chondroitin sulphate, such as the sodium salt of chondroitin sulphate.
  • the source of the chondroitin is preferably chicken.
  • a composition (C) according to the invention was prepared in the form of a syrup (total volume of 100 ml) comprising the following ingredients: - Lyophilised Aloe vera gel (a): 0.25 g - Sodium hyaluronate (b): 0.23 g - Honey (c): 25 g - Fructose: 23.8 g - Hydroxypropyl methylcellulose: 3 g - Benzoates (preservatives): 0.15 g - Flavourings: 0.3 g - Thickener: 0.1 g - Purified water: q.s. to 100 ml
  • a composition (C) according to the invention was prepared in the form of a syrup (total volume of 100 ml) comprising the following ingredients: - Lyophilised Aloe vera gel (a): 0.25 g - Sodium hyaluronate (b): 0.23 g - Honey (c): 25 g - Chondroitin sulphate sodium (d): 2.8 g - Fructose: 23.8 g - Hydroxypropyl methylcellulose: 3 g - Benzoates (preservatives): 0.15 g - Flavourings: 0.3 g - Thickener: 0.1 g - Water: q.s. to 100 ml
  • a composition (C) according to the invention was prepared in the form of a syrup (total weight 100 g) comprising the following ingredients: - Lyophilised Aloe vera gel (a): 0.21 g - Sodium hyaluronate (b): 0.24 g - Honey (c): 21 g - Chondroitin sulphate sodium (d): 2.3 g - Fructose: 6.2 g - Potassium/dipotassium phosphate buffer 2.1 g - Sodium hydroxide 0.15 g - Benzoates (preservatives): 0.15 g - Xanthan gum 0.25 g - Flavourings: 0.3 g - Maltodextrins 11.6 g - Thickener (guar flour) 0.2 g - Water: 55 g - Other excipients: q.s. to 100 g
  • compositions of examples 1, 2 and 3 were orally administered to subjects affected by gastroesophageal reflux disease (GERD), diagnosed through endoscopic analysis.
  • GFD gastroesophageal reflux disease
  • liquid composition (C) in the embodiment of the above-referred formulation (liquid composition (C)), the aforesaid invention lends itself to being used in subjects of all ages, from newborns to the elderly.
  • the liquid composition (C) of the present invention (which comprises a mixture which comprises or, alternatively, consists of (a), (b), (c) and/or (d)): is preferably an association (mixture) of Chondroitin Sulphate, Hyaluronic acid, Aloe and Honey, endowed with the following properties:
  • the liquid composition (C) comprising a mixture which comprises or, alternatively, consists of (a), (b), (c) and/or (d) is in the form of a solution or syrup or sachets and enables better contact of the individual components/substances with the oral-pharyngeal-laryngeal-esophageal wall, favouring the protection, lubrication and repair thereof:
  • Preferred intended uses of the aforesaid liquid composition (C) comprising a mixture which comprises or, alternatively, consists of (a), (b), (c) and/or (d) are: as an adjuvant for the symptomatic treatment of gastroesophageal reflux disease; or for use in a preventive and/or curative action against: (i) lesions of the oral cavity (e.g. tongue and palate) and of the pharyngeal-laryngeal-esophageal tract; (ii) mucositis; (iii) aphthae and/or aphthoid lesions.
  • the present invention relates to a liquid composition (C) which comprises a combination or an association or a mixture which comprises or, alternatively, consists of: (a) Aloe vera gel; (b) hyaluronic acid; and (c) honey and, optionally, (d) chondroitin sulphate or a salt thereof, preferably a sodium salt, for use as an adjuvant for the symptomatic treatment of gastroesophageal reflux disease; or for use in a preventive and/or curative treatment against: (i) lesions of the oral cavity (e.g.
  • the model used was Reconstituted Human Esophageal Epithelium, produced by Episkin ®, Lyons (F)
  • the time of contact with the esophageal mucosa was 15 min (time for stabilisation of the deposit of products at the level of the mucosa) for all protocols. The time was extended to 1h after elimination of the excess of the residual volume.
  • the products (100 ⁇ L) dispersed in saline solution were applied for 15 minutes and after removal of the excess for up to 1h on the surface of the esophageal epithelium at a temperature of 32°C; then, without removing it, 100 ⁇ L of a 0.5%/0.5 cm 2 solution of caffeine and 1 mg caffeine/cm 2 (in an acidic or neutral solution) were applied. During this period the receptor fluid below the insert was represented by a saline solution.
  • the receptor fluids were recovered at 15 min, 1 h and 2 h in the basolateral compartment and subsequently analysed for the content of caffeine with the HPLC technique.
  • the tissues were then used to carry out a Lucifer Yellow (LY) assay to confirm the integrity and permeability of the barrier.
  • Lucifer yellow is a fluorescent marker impermeable to the cell membrane.
  • a surface abrasion/acid pH treatment was applied on the surface in order to induce and simulate the loss of continuity of the mucosa damaged by lesions due to acid reflux. Abrasions result in a reduction in electrical resistance (TEER) and an increase in the release of LDH and loss of connection of the cells of the surface epithelium.
  • TEER electrical resistance
  • the tissues were used for biotin marking with an immunohistochemical technique, which distinguishes the permeable parts of the tissue from the non-permeable ones, which therefore, have an intact barrier function.
  • TGF Transforming Growth Factor
  • Transepithelial electrical resistance is a direct measurement of the functionality of the barrier of epithelial tissues: it reflects the global resistance of the tissue due both to its thickness and structure, since it reflects the integrity of intercellular contacts at the level of the tight junctions which oppose the penetration of external substances.
  • lactate dehydrogenase is normally present in the cytoplasm and cannot be found outside cells except as a result of damage to the cell membrane.
  • a histological and complementary immunohistochemical analysis make it possible to visualise the interaction of the product with living tissue and the structure of the proteins of tight junctions (zonulin-1 and occludin), which are essential for maintaining the barrier intact.

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Claims (10)

  1. Composition liquide (C) comprenant un mélange qui comprend ou, en variante, consiste en, les composants/ substances qui suivent :
    (a) un gel d'Aloe vera ;
    (b) un acide hyaluronique ou un sel de celui-ci ; et
    (c) un miel et, éventuellement, des additifs et/ou excipients de qualité pharmaceutique ou alimentaire.
  2. Composition (C) selon la revendication 1, dans laquelle l'acide hyaluronique a un poids moléculaire compris entre 400 et 900 kDa, de préférence entre 600 et 800 kDa.
  3. Composition (C) selon l'une des revendications précédentes, dans laquelle ledit mélange comprend en outre :
    (d) un sel de chondroïtine, de préférence de sulfate de chondroïtine, sous la forme d'un sel sodique de sulfate de chondroïtine.
  4. Composition (C) selon l'une des revendications précédentes, dans laquelle le gel d'Aloe vera est un gel de feuille intérieure lyophilisé.
  5. Composition (C) selon l'une des revendications précédentes, dans laquelle ledit mélange comprend ou, en variante, consiste en :
    (a) en une quantité comprise entre 0,1 et 0,5 % ;
    (b) en une quantité comprise entre 0,1 et 0,5 % ;
    (c) en une quantité comprise entre 10 et 40 % ; et
    (d), s'il est présent, en une quantité comprise entre 1 et 4 %,
    dans laquelle toutes les quantités sont en poids par rapport au poids total de (c).
  6. Composition (C) selon l'une des revendications précédentes, comprenant, pour 100 ml de (C) :
    (a) en une quantité comprise entre 150 et 300 mg ;
    (b) en une quantité comprise entre 100 et 300 mg ;
    20 à 30 g de (c) ; éventuellement
    2 à 3 g de (d).
  7. Dispositif médical comprenant la composition (C) selon l'une quelconque des revendications précédentes.
  8. Composition comprenant un mélange ou une association ou une combinaison qui comprend ou, en variante, consiste en :
    (a) un gel d'Aloe vera ;
    (b) un acide hyaluronique ; et
    (c) un miel et, éventuellement,
    (d) du sulfate de chondroïtine ou un sel de celui-ci, de préférence un sel sodique ; et éventuellement des additifs et/ou excipients de qualité pharmaceutique ou alimentaire, ladite composition étant
    - destinée à être utilisée dans le traitement et/ou la prévention d'un reflux gastro-œsophagien, laquelle utilisation comprend l'administration de (a), (b) et (c) à un sujet dans n'importe quel ordre ou simultanément, ou
    - destinée à être utilisée en tant qu'adjuvant pour le traitement symptomatique d'un reflux gastro-œsophagien ; ou
    - destinée à être utilisée dans un traitement préventif et/ou curatif contre : (i) des lésions de la cavité orale (par exemple de la langue et du palais) et des voies pharyngées laryngées œsophagiennes ; (ii) une mucosite ; et/ou (iii) des aphtes et/ou des lésions aphtoïdes, laquelle utilisation comprend l'administration de (a), (b), (c) et/ou (d) à un sujet dans n'importe quel ordre ou simultanément.
  9. Composition pour une utilisation selon la revendication 8, dans laquelle ladite utilisation comprend l'administration de a), b) et c) simultanément, de préférence dans une seule composition.
  10. Composition (C) selon au moins une des revendications 1 à 6, ayant une des trois compositions suivantes : composition 1 : - gel d'Aloe vera lyophilisé (a) : 0,25 g - hyaluronate de sodium (b) : 0,23 g - miel (c) : 25 g - fructose : 23,8 g - hydroxypropylméthylcellulose : 3 g - benzoates (conservateurs) : 0,15 g - arômes : 0,3 g - épaississant : 0,1 g - eau purifiée : q.s. à 100 ml
    composition 2 : - gel d'Aloe vera lyophilisé (a) : 0,25 g - hyaluronate de sodium (b) : 0,23 g - miel (c) : 25 g - sulfate de chondroïtine sodique (d) : 2,8 g - fructose : 23,8 g - hydroxypropylméthylcellulose : 3 g - benzoates (conservateurs) : 0,15 g - arômes : 0,3 g - épaississant : 0,1 g - eau : q.s. à 100 ml
    composition 3 : - gel d'Aloe vera lyophilisé (a) : 0,21 g - hyaluronate de sodium (b) : 0,24 g - miel (c) : 21 g - sulfate de chondroïtine sodique (d) : 2,3 g - fructose : 6,2 g - tampon phosphate de potassium/dipotassium : 2,1 g - hydroxyde de sodium : 0,15 g - benzoates (conservateurs) : 0,15 g - gomme xanthane 0,25 g - arômes : 0,3 g - maltodextrines : 11,6 g - eau : 55 g - autres excipients : q.s. à 100 g
EP17797183.5A 2016-10-10 2017-10-10 Composition liquide destinée à être utilisée dans le traitement de reflux gastro-oesophagien Active EP3522904B1 (fr)

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IT102016000101413A IT201600101413A1 (it) 2016-10-10 2016-10-10 Composizione liquida per uso nel trattamento del reflusso gastroesofageo
PCT/IB2017/056254 WO2018069832A1 (fr) 2016-10-10 2017-10-10 Composition liquide destinée à être utilisée dans le traitement de reflux gastro-œsophagiens

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IT201900008409A1 (it) * 2019-06-07 2020-12-07 Vivatis Pharma Gmbh Individuazione e selezione di un materiale di partenza vegetale di condroitina solfato e acido ialuronico vegetali, e trasformazione di tale materiale di partenza vegetale per l’ottenimento di ingredienti per utilizzo in alimenti, integratori, dispositivi medici o farmaci
IT202000022477A1 (it) * 2020-09-23 2022-03-23 Sofar Swiss Sa Composizioni comprendenti una condroitina vegetale o un suo analogo e loro uso nel trattamento disturbi della mucosa del tratto orale, faringo-laringeo e/o gastro-esofageo
IT202000022471A1 (it) * 2020-09-23 2022-03-23 Sofar Swiss Sa Composizioni comprendenti una condroitina vegetale o un suo analogo e loro uso nel trattamento disturbi della mucosa del tratto orale, faringo-laringeo e/o gastro-esofageo
IT202100021992A1 (it) * 2021-08-27 2023-02-27 Neilos S R L Composizione per la prevenzione e/o il trattamento delle patologie gastriche ed esofagee
IT202100021995A1 (it) * 2021-08-27 2023-02-27 Neilos S R L Composizione per la prevenzione e/o il trattamento delle patologie gastriche ed esofagee

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IT201600101413A1 (it) 2018-04-10
US20220265701A1 (en) 2022-08-25
ES2900565T3 (es) 2022-03-17
DK3522904T3 (da) 2021-12-06
US11690867B2 (en) 2023-07-04
PL3522904T3 (pl) 2022-02-07
PT3522904T (pt) 2021-12-13
US11337992B2 (en) 2022-05-24
EP3522904A1 (fr) 2019-08-14
HUE057257T2 (hu) 2022-05-28
US20190262388A1 (en) 2019-08-29
WO2018069832A1 (fr) 2018-04-19

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